Adrenal disorders: Difference between revisions
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{{familytree | | C01 | | C02 | | C03 | | C04 | | C05 | |C01=[[Congenital adrenal hyperplasia]]|C02=[[Adrenal disorders#Classification|Aldosterone disorders]]|C03=[[Adrenal disorders#Classification|Cortisol disorders]]|C04=[[Adrenal insufficiency]]|C05=[[Adrenal Tumors]]|}} | {{familytree | | C01 | | C02 | | C03 | | C04 | | C05 | |C01=[[Congenital adrenal hyperplasia]]|C02=[[Adrenal disorders#Classification|Aldosterone disorders]]|C03=[[Adrenal disorders#Classification|Cortisol disorders]]|C04=[[Adrenal insufficiency]]|C05=[[Adrenal Tumors]]|}} | ||
{{familytree | | |!| | | |!| | | |!| | | |!| | | |!| | | | |}} | {{familytree | | |!| | | |!| | | |!| | | |!| | | |!| | | | |}} | ||
{{familytree | | D01 | | C02 | | C03 | | C04 | | C05 | | |D01=[[21-hydroxylase deficiency]]<br> [[11β-hydroxylase deficiency]] <br> [[17 alpha-hydroxylase deficiency]] <br> [[3 beta-hydroxysteroid dehydrogenase deficiency]] <br> [[Cytochrome P450-oxidoreductase (POR) deficiency (ORD)]] <br> [[Lipoid congenital adrenal hyperplasia]]|C02=[[Primary hypertaldosteronism]] <br> [[Hypoaldosteronsim]]|C03=[[Cushing's syndrome]]|C04=[[Addison's disease]]|C05=[[Incidentiloma]] <br> [[pheocromocytoma]]}} | {{familytree |boxstyle=text-align: left; | | D01 | | C02 | | C03 | | C04 | | C05 | | |D01= • [[21-hydroxylase deficiency]]<br> •[[11β-hydroxylase deficiency]] <br> •[[17 alpha-hydroxylase deficiency]] <br> •[[3 beta-hydroxysteroid dehydrogenase deficiency]] <br> •[[Cytochrome P450-oxidoreductase (POR) deficiency (ORD)]] <br> •[[Lipoid congenital adrenal hyperplasia]]|C02= •[[Primary hypertaldosteronism]] <br> •[[Hypoaldosteronsim]]|C03=[[Cushing's syndrome]]|C04=[[Addison's disease]]|C05= •[[Incidentiloma]] <br> •[[pheocromocytoma]]}} | ||
{{familytree/end}} | {{familytree/end}} | ||
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Revision as of 20:00, 30 August 2017
Adrenal disorders Main Page |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Usama Talib, BSc, MD [2]
Overview
Classification